CN108328596A - A kind of carbon sponge and preparation method thereof and pressure sensor - Google Patents
A kind of carbon sponge and preparation method thereof and pressure sensor Download PDFInfo
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- CN108328596A CN108328596A CN201710302314.0A CN201710302314A CN108328596A CN 108328596 A CN108328596 A CN 108328596A CN 201710302314 A CN201710302314 A CN 201710302314A CN 108328596 A CN108328596 A CN 108328596A
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01L—MEASURING FORCE, STRESS, TORQUE, WORK, MECHANICAL POWER, MECHANICAL EFFICIENCY, OR FLUID PRESSURE
- G01L5/00—Apparatus for, or methods of, measuring force, work, mechanical power, or torque, specially adapted for specific purposes
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- C01B2204/20—Graphene characterized by its properties
- C01B2204/22—Electronic properties
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- C01B2204/00—Structure or properties of graphene
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- C01P2006/16—Pore diameter
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- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
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- C01P2006/40—Electric properties
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Abstract
A kind of carbon sponge of present invention offer and preparation method thereof and pressure sensor, belong to nano materials research field.A kind of method with the compressible hyperelastic carbon sponge of omnidirectional being made up of " adobe " structure amorphous carbon and graphene is prepared, including:Small molecular organic acid additive and graphene oxide are distributed in solvent and form graphene oxide and additive mixing dispersion solution;Mixed solution is dried, the graphene oxide sponge containing additive is obtained;High-temperature heat treatment graphene oxide containing additive sponge under inert gas protection obtains carbon sponge.Obtained carbon sponge have the compressible super-elasticity of omnidirectional, omnidirectional can reply compressibility, high intensity and high conductivity.The invention further relates to a kind of tactile based on the sponge and pressure sensors and preparation method thereof.
Description
Technical field
The present invention relates to technical field of nano material, more particularly to a kind of carbon sponge and preparation method thereof and pressure sensing
Device.
Background technology
Sponge is a kind of porous material with favorable elasticity, and aeroge is referred to as " super sponge ".Aeroge have than
The features such as surface area is big, porosity is big, density is small, thermal conductivity is low is urged in electronics industry, aerospace, the energy, chemical industry, industry
There is huge application potential in the fields such as change, environmental protection.Common aeroge is aerosil, be widely used in it is heat-insulated,
The fields such as sound insulation, damping.In recent years, full carbon aerogels especially graphene aerogel obtains the wide of scientific research personnel and industrial quarters
General concern.Since graphene is with high conductivity (1 × 106S/m), high-modulus (1TPa), high intensity (130GPa) Gao Bibiao
Area (2630m2/ g) etc. excellent properties New Two Dimensional material, the full carbon aerogels constituted based on graphene are expected to have both
The excellent properties of graphene and aeroge realize the preparation of high resiliency, high intensity, the high super sponge of conductivity.
Chemical vapor deposition and oxidation-reduction method are the main methods realized graphene and prepared on a large scale, with both methods
Based on developed the method that two major classes prepare graphene sponge:Template vapour deposition process and solution self-assembly method.Template gas phase
Sedimentation first passes through chemical vapor deposition on the three-dimensional porous materials such as nickel foam or silica sponge and goes out continuous tubulose stone
Black alkene three-dimensional network, then perforated substrate is etched away, obtain graphene sponge after being then further dried and being heat-treated.This side
Although graphene sponge crystallinity prepared by method is high, electricity and excellent in mechanical performance, its microstructure depend on substrate
Porous material is not easy to regulate and control it, while being difficult to overcome and complicated technology and excessive temperature is needed to be heat-treated (2250 DEG C) band
The high-cost problem come.Solution self-assembly method is compared with template vapour deposition process, without depositing template, so its structure and property
Matter is easy to, while not needing the treatment temperature of complicated technique and superelevation, at low cost, is more suitable for industrializing.But it is existing
The carbon sponge mechanics and electric property that some solution self-assembly methods obtain are bad, can not be comparable with template vapour deposition process.I.e.
Make to fix graphene network by composite carbon nanometer tube or macromolecule in solution self-assembly method, obtained sponge does not also have
The compressible super-elasticity of standby omnidirectional, omnidirectional can reply compressibility, while intensity and electric conductivity is not high.The omnidirectional is compressible super
Elasticity or omnidirectional can reply compressibility has super-elasticity or compressed recession along any direction of its three-dimensional system of coordinate (X-Y-Z)
60% of reduction length or more property can be returned to when falling pressure.
In conclusion there has been no the good preparations of low cost, controllability, and there is the compressible super-elasticity of omnidirectional, omnidirectional can return at present
The report of the carbon sponge of compound compression, high intensity and high conductivity.
And have the compressible super-elasticity of omnidirectional, omnidirectional can reply the carbon sponge of compressibility, high intensity and high conductivity not only
It plays a decisive role in constructing the electronics devices such as flexible battery, ultracapacitor, sensor, the brake of Novel pressure-resistant contracting,
And to carbon biological tissue holder of the future development based on carbon sponge, ultralight mechanical damping porous material and it is ultralight it is heat-insulated/every
Sound porous material is most important.Therefore, develop a kind of preparation process is simple and direct, controllability is good, prepare have the compressible superlastic of omnidirectional
Property, high intensity and high conductivity carbon sponge method have important scientific meaning and application value.
Invention content
The purpose of the present invention is in view of the deficiencies of the prior art, exploitation is a kind of to have the compressible super-elasticity of omnidirectional, omnidirectional can
Reply compressibility, high intensity and high conductivity carbon sponge, and provide preparation method.
Another object of the present invention is:Based on it is this have the compressible super-elasticity of omnidirectional, omnidirectional can reply compressibility, height
The carbon sponge of intensity and high conductivity, provide it is a kind of can the low and highly sensitive tactile of omnidirectional's detection pressure, detection limit and
Pressure sensor.
Particularly, carbon sponge provided by the invention is a kind of composition, it is characterized in that:By graphene or the oxygen of partial reduction
Graphite alkene and amorphous carbon are constructed and to be formed by " brick mud " structure;" the brick mud " is if structure refers to the stone by single layer or dried layer
Black alkene or the graphene oxide of partial reduction are used as " brick ", amorphous carbon is coated as " mud " or part coat the graphene or
The graphene oxide of partial reduction, so that graphene or the graphene oxide of partial reduction are connected with amorphous carbon into similar
The porous network shape composite construction of " brick mud " structure;The weight percent of its component is:Graphene or the oxidation stone of partial reduction
Black alkene 0.1-99.9%, amorphous carbon 0.1%-99.9%.
Carbon sponge is macroscopically porous foam shape.Shape, size and dimension are unlimited.It is made of carbon and oxygen element, no
Containing other elements.Density can be less than 0.25mg/cm3.Pore size range is unlimited, it is therefore preferable to 1.5nm-550 μm.Along difference
Direction all has excellent elasticity and can reply compressibility, that is, compressibility can be replied by having the compressible super-elasticity of omnidirectional and omnidirectional.
Compressive strength can be more than 400kPa, and conductivity can be more than 90S/m.
Further, the carbon sponge formed by graphene and amorphous carbon, consisting of carbon;By partial reduction
Graphene oxide and amorphous carbon formed the carbon sponge, consisting of oxygen and carbon;Wherein, the oxygen of the carbon sponge
When Elements Atom percentage≤1%, the carbon sponge is full carbon sponge.
Preferably, carbon sponge oxygen element atomic percent >=0.01%, remaining all carbon.
Preferably, full carbon sponge oxygen element atomic percent >=0.01% and≤1%, remaining all carbon.
Further, component ratio is arbitrarily adjustable in carbon sponge.
Optionally, the atomic percent of oxygen element can be controlled in 60%-50% in the component of carbon sponge, remaining is complete
Portion is carbon.
Optionally, the atomic percent of oxygen element can be controlled in 50%-20% in the component of the carbon sponge,
Remaining all carbon.
Optionally, the atomic percent of oxygen element can be controlled in 20%-10% in the component of the carbon sponge,
Remaining all carbon.
Optionally, the atomic percent of oxygen element can be controlled in 10%-5% in the component of the carbon sponge,
Remaining all carbon..
Optionally, the atomic percent of oxygen element can be controlled in 5%-3% in the component of the carbon sponge,
Remaining all carbons.
Optionally, the atomic percent of oxygen element can be controlled in 3%-1% in the component of the carbon sponge,
Remaining all carbons.
Optionally, the atomic percent of oxygen element can be controlled in 0.1%- in the component of the full carbon sponge
1%, remaining all carbon.
Optionally, the atomic percent of oxygen element can be controlled in 0%- in the component of the full carbon sponge
0.6%, remaining all carbon.
Optionally, the atomic percent of oxygen element can be controlled in 0%- in the component of the full carbon sponge
0.1%, remaining all carbon.
Optionally, the atomic percent of oxygen element can be controlled in 0.1%- in the component of the carbon sponge
60%, remaining all carbon.
Further, the carbon sponge has compressible super-elasticity, can reply compressibility and electric conductivity;
Particularly, there is the carbon sponge the compressible super-elasticity of omnidirectional, omnidirectional can reply compressibility and electric conductivity;
Wherein, the compressible super-elasticity refers to the sponge can be restored to when removing pressure after the compression of its any direction
Original length;The compressibility of replying can restore original length when to refer to the sponge remove pressure after the compression of its any direction
60% or more of degree.
The strain of the compressible recovery of the compressible super-elasticity of omnidirectional and omnidirectional of carbon sponge provided by the invention exists in range
It is adjustable in 0.1-99.9%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 0.1-
20%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 20-40%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 40%-
60%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 60-80%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 70-90%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 90-
95.9%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 96-
99.9%.
Optionally, the strain model of the compressible recovery of the compressible super-elasticity of omnidirectional and omnidirectional of carbon sponge provided by the invention
It encloses including 98.5-99.9%.
Carbon sponge provided by the invention is ultralight, and density can be less than 0.5mg/cm3。
The density of carbon sponge provided by the invention is adjustable in a certain range;
Optionally, the density range of the carbon sponge includes being less than 0.25mg/cm3。
Optionally, the density range of the carbon sponge includes 0.25-0.5mg/cm3。
Optionally, the density range of the carbon sponge includes being more than 0.25mg/cm3。
Optionally, the density range of the carbon sponge includes being more than 0.5mg/cm3。
Optionally, the density range of the carbon sponge includes 0.51-1mg/cm3。
Optionally, the density range of the carbon sponge includes 1-5mg/cm3。
Optionally, the density range of the carbon sponge includes 0.5-3mg/cm3。
Optionally, the density range of the carbon sponge includes 5-15mg/cm3。
Optionally, the density range of the carbon sponge includes 15-30mg/cm3。
Optionally, the density range of the carbon sponge includes 30-50mg/cm3。
Optionally, the density range of the carbon sponge includes 40-50mg/cm3。
Optionally, the density range of the carbon sponge includes 50-100mg/cm3。
Optionally, the density range of the carbon sponge includes 100-200mg/cm3。
The pore diameter range of carbon sponge provided by the invention is adjustable in a certain range;It preferably, can in 1.5nm-550 μm
It adjusts.
Optionally, the pore diameter range of the carbon sponge includes 1.5nm-100nm.
Optionally, the pore diameter range of the carbon sponge includes 1nm-100nm.
Optionally, the pore diameter range of the carbon sponge includes 100nm-10 μm.
Optionally, the pore diameter range of the carbon sponge includes 10 μm -50 μm.
Optionally, the pore diameter range of the carbon sponge includes 50 μm -200 μm.
Optionally, the pore diameter range of the carbon sponge includes 200 μm -250 μm.
Optionally, the pore diameter range of the carbon sponge includes being more than 250 μm.
Further, carbon sponge provided by the invention has the characteristics that ultralight and high intensity.Carbon sponge can be born to reach itself
Several weights of weight compress and keep its structural intergrity.The time equal energy of density, graphene and amorphous carbon ratio, heat treatment
The ratio of (finger pressure contracting can be born and keep its structural intergrity) weight quality and own wt that can be born of regulation and control sponge.
Preferably, the ratio of the weight quality and own wt that can bear of carbon sponge is up to 150,000 or more.
Preferably, the ratio of the weight quality and own wt that can bear of the carbon sponge is less than or equal to 0.8 ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge includes 0.8 ten thousand -5
Ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge includes 5.1 ten thousand -10
Ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge includes 100,000-20
Ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge up to 100,000 with
On.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge includes 200,000-50
Ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge includes 300,000-50
Ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge up to 300,000 with
On.
Further, the carbon sponge is in macroscopically the porous foam shape of random geometry;The carbon sponge can be added
Work is cut into random geometry.
Further, the shape of the carbon sponge includes sphere, cube, cylinder, the polygon cylinder of rule;It does not advise
Solid then;Thin slice, the film of arbitrary shape;Fiber and nano wire.
Further, unlimited in carbon sponge dimension, including three-dimensional, such as the block shape of random geometry;Two dimension, such as nanometer
Piece, film;It is one-dimensional, as nanofiber, nanometer are linear;Zero dimension, such as micron ball, nanosphere.
Further, described " brick mud " structure refers to by single layer to several layers of graphenes or the graphite oxide of partial reduction
Alkene lamella is used as " brick ", and the amorphous carbon that pyrolysis additive generates is porous as similar " brick mud " structure made of " mud " linking
Network-like composite construction;The weight percent of its component is:Graphene or the graphene oxide 0.1-99.9% of partial reduction, nothing
Shape carbon 0.1%-99.9%.
Preferably, the graphene 10%-90% in carbon sponge, amorphous carbon 10%-80%.
Preferably, the graphene 50%-80% in carbon sponge, amorphous carbon 20%-50%.
The present invention also provides a kind of preparation methods of the compressible super-elasticity carbon sponge of omnidirectional, include the following steps:
Additive and graphene oxide are distributed in solvent and form graphene oxide and additive mixed solution;
The mixed solution is dried, the graphene oxide sponge containing additive is obtained;
High-temperature heat treatment graphene oxide containing additive sponge under inert gas protection obtains carbon sponge or full carbon sea
It is continuous.
Further, the additive is one or more of small molecular organic acid;
Preferably, the additive is ascorbic acid, citric acid, tartaric acid, lactic acid, one or more of benzoic acid.
Further, the solvent is the solvent for disperseing the additive and the graphene oxide, commonly
For water and organic solvent;Preferably, the solvent be water, ethyl alcohol, acetone, dimethylformamide, one kind in carbon tetrachloride or
Several mixed liquors.
Further, the drying means for the dry mixed solution containing additive and graphene oxide is unlimited;
Preferably, the drying means for the dry mixed solution containing additive and graphene oxide is that freezing is dry
One or more of dry, supercritical drying, vacuum drying and normal pressure heated drying.
Further, the temperature range of high-temperature heat treatment is unlimited, and the time of high-temperature heat treatment is unlimited.Preferably, high warm
The temperature range of processing is 200-2500 DEG C.Preferably, the time of high-temperature heat treatment is 0.1-100h.
Further, in the high-temperature heat treatment process, using higher heat treatment temperature and longer heat treatment when
Between be conducive to obtain higher reducing degree and the carbon sponge compared with low oxygen content, even without the full carbon sponge of oxygen.
Preferably, the carbon sponge includes the carbon sponge slightly restored, and the atomic percent proportion of oxygen element is 10%-
60%.
Preferably, the carbon sponge includes the carbon sponge of moderate reduction, and the atomic percent proportion of oxygen element is 1%-
10%.
Preferably, the carbon sponge includes the carbon sponge of height reduction, and the atomic percent proportion of oxygen element is 0.5%-
1%.
Preferably, the carbon sponge includes the carbon sponge of high degree reduction, and the atomic percent proportion of oxygen element is≤
0.5%.
Further, the carbon sponge have the compressible super-elasticity of omnidirectional, omnidirectional can reply compressibility, high intensity and it is high
Electric conductivity.
Compared to the prior art the present invention has the advantage that:
(1) compared with template vapour deposition process, the method that the present invention prepares carbon sponge does not need the step of chemical vapor deposition
Suddenly, therefore complicated chemical vapor depsotition equipment is not needed, preparation method is simple and direct, at low cost.Template vapour deposition process utilizes more
Mesoporous metal is as substrate deposition graphene, so its microstructure depends on the structure of porous metals, is formed for tubular graphene alkene
Network;And the composite construction that " brick mud " structural carbon sponge prepared by the present invention is made of sheet graphene and amorphous carbon
Network can also be obtained by curling graphene film stratiform in the case of but unclosed be formed at tubular graphene alkene and amorphous carbon
Composite construction carbon sponge network;The microstructure and constituent of the two have very big difference.
(2) compared with existing solution self-assembly method, " brick mud " structural carbon sponge prepared by the present invention be by graphene and
The constituent of pyrogenous origin amorphous carbon composition and existing solution self-assembly method, i.e., by macromolecule and graphene, graphite
Graphene is different with carbon nanotube or only for alkene.Due to strong between amorphous carbon and graphene in " brick mud " structure of the present invention
The synergistic effect that generates of π-π interaction, keep prepared carbon sponge porous network firmer, it is compressible to be provided with omnidirectional
Super-elasticity and omnidirectional can reply compressibility, and intensity and conductivity are far longer than sponge prepared by existing solution self-assembly method.
(3) with the method for pyrolysis chitosan and graphene oxide mixture (Nature Communications, 2016,7,
12920) it compares, carbon sponge element group prepared by the present invention becomes carbon and part oxygen element, and is pyrolyzed chitosan and oxidation
The composition of sponge prepared by the method for graphene mixture not only contains carbon and oxygen element and also contains 6% nitrogen, so
The two constitution element component difference is very big.The additive that present invention preparation sponge uses is the organic acid of small molecule, and pyrolysis shell
The polymer chitosan that the method for glycan and graphene oxide mixture uses has difference substantially.The preparation process of the present invention
In mixing liquid need not be processed with liquid nitrogen.Carbon sponge network prepared by the present invention is firmer, has omnidirectional's super-elasticity
Compressibility can be replied with omnidirectional, intensity and conductivity are far longer than the sponge of above method preparation.
(4) the carbon sponge of the composite network structure of the graphene and amorphous carbon with " adobe structure " described in, has
The compressible super-elasticity of omnidirectional, omnidirectional can reply compressibility, high intensity and high conductivity, can be used to construct Novel pressure-resistant contracting it is soft
The electronics devices such as property battery, ultracapacitor, sensor, brake.Also carbon biological tissue holder, ultralight machinery resistance be can be used as
Buddhist nun's porous material and ultralight heat/sound insulation porous material.
The present invention provides a kind of pressure sensor, can be used for detecting the pressure of carbon aerogels any direction;Its structure is:Such as
Electric signal measurement device between the preceding carbon aerogels, electrode and the measurement electrode and carbon aerogels.Aeroge and
There are conductive silver glues between electrode, for eliminating influence of the contact resistance for signal.
The wherein pressure sensor, using bulk resistor effect as its sensor mechanism, detection power range is big, sensitivity
Higher, low energy consumption, and stability is good, the pressure on detectable any direction.
The present invention also provides a kind of tactile and pressure sensor, it can be used for detecting the tactile and pressure of carbon sponge any direction
Power;Its structure is:The electrode and measure between the electrode and carbon sponge that foregoing carbon sponge, carbon sponge surface contact
The electric signal measurement device of resistance value.
Tactile provided by the invention and pressure sensor be based on above-mentioned carbon sponge it is a kind of can omnidirectional's detection pressure, visit
Survey the low and highly sensitive sensor of lower limit.
Optionally, there is no any binders or mechanical connection to fix for the contact interface between electrode and carbon sponge.
Further, the electric signal of the output of sensor is unlimited.In the particular embodiment, the electric signal of sensor output
Can be electric current, voltage, resistance.
Tactile provided by the invention and pressure sensor, using interface contact resistance effect rather than body piezoresistive effect conduct
Sensor mechanism, detection power lower limit is up to less than or equal to 15Pa (touching gently in the corresponding people's tactiles of 10Pa or so), sensitivity
It is adjustable;100/kPa is preferably may be up to, energy consumption is adjustable;Preferably, 30 μ W can be less than.
Further, the detection limit and work of the pressure sensor are controlled as work materials by using different sponges
Make range.
Optionally, the sensor includes being directed to small pressure, and detection limit is less than or equal to the touch sensor of 15Pa.
Optionally, the sensor includes being directed to middle pressure, and detection limit is less than or equal to the touch sensor of 50Pa.
Optionally, the sensor can also include being directed to smaller pressure, and working range passes for 15Pa-200Pa pressure
Sensor.
Optionally, the sensor includes being directed to middle pressure, and working range is the pressure sensing of 200Pa-10kPa
Device.Can also include being directed to middle pressure, working range is the pressure sensor of 100Pa-5kPa.
Optionally, the sensor includes being directed to big pressure, and working range is the pressure sensor more than 10kPa.
Optionally, the sensor includes being directed to big pressure, and working range is the pressure sensor more than 100kPa.
Preferably, the tactile and pressure sensor use conductive carbon material as electrode and conducting wire, obtained sensing
Device is full carbon tactile and pressure sensor.
Further, the full carbon tactile and pressure sensor Ultra light-weight.
Further, the full carbon tactile and pressure sensor can work under extreme environment.Operating temperature model
Width is enclosed, can be worked normally under extremely low temperature;The corrosion of acid and alkali resistance and salt.
Compared to the prior art the present invention has the advantage that:
It is described based on the compressible super-elasticity of omnidirectional, high intensity and the carbon sponge of high conductivity can detect along arbitrary
The tactile and pressure sensor of square upward pressure not only expand the working range of sensor and improve ability to work, reduce
The cost of layout of sensor.Its detection limit is low, high sensitivity, is suitable as the monitoring of health signal and mechanical bionic hand
Touch sensor.Particularly, it when using conductive carbon materials such as carbon nanotube or graphenes as electrode and conducting wire, can prepare
The sensor of full carbon.The sensor of full carbon has the characteristics that wide light weight, operating temperature range, acid and alkali-resistance and salt corrosion, is navigating
The special occasion for needing tactile and pressure detection such as empty space flight, strong corrosive environment is with a wide range of applications.
According to the following detailed description of specific embodiments of the present invention in conjunction with the accompanying drawings, those skilled in the art will be brighter
The above and other purposes of the present invention, advantages and features.
Description of the drawings
Some specific embodiments that the invention will be described in detail by way of example and not limitation with reference to the accompanying drawings hereinafter.
Identical reference numeral denotes same or similar component or part in attached drawing.It should be appreciated by those skilled in the art that these
What attached drawing was not necessarily drawn to scale.In attached drawing:
Fig. 1 is the schematic diagram according to the carbon sponge of different shapes of the present invention;
Fig. 2 is the micro image according to the carbon sponge of one embodiment of the present of invention;
Load-deformation curve when Fig. 3 is according to the carbon sponge of one embodiment of the present of invention along a certain be compressed axially;
Load-deformation curve when Fig. 4 is according to the carbon sponge of one embodiment of the present of invention along another be compressed axially;
Load-deformation curve when Fig. 5 is according to the carbon sponge of one embodiment of the present of invention along another be compressed axially;
Fig. 6 is the load-deformation curve according to the compression of the carbon sponge of one embodiment of the present of invention;
Fig. 7 is to be passed according to the tactile and pressure of tactile and pressure on any direction that can detect of one embodiment of the present of invention
The schematic cross-section of sensor;
Fig. 8 is to be passed according to the tactile and pressure of tactile and pressure on any direction that can detect of one embodiment of the present of invention
The schematic cross-section of sensor;
Fig. 9 is the tactile and pressure that can detect tactile and pressure on eight different directions according to one embodiment of the present of invention
The schematic cross-section of force snesor;
Figure 10 be according to one embodiment of the present of invention can detect on six different directions the tactile of tactile and pressure and
The schematic cross-section of pressure sensor;
Figure 11 be according to one embodiment of the present of invention can detect on eight different directions the tactile of tactile and pressure and
The schematic cross-section of pressure sensor;
Figure 12 be according to one embodiment of the present of invention can detect on six different directions the tactile of tactile and pressure and
The schematic cross-section of pressure sensor;
Figure 13 be according to one embodiment of the present of invention can detect on two different directions the tactile of tactile and pressure and
The schematic diagram of pressure sensor.
Figure 14 is a kind of flow diagram of the preparation method of the carbon sponge of embodiment of the present invention.
Specific implementation mode
The present invention is specifically described by embodiment, the present embodiment is served only for doing further the present invention
It is bright, it should not be understood as limiting the scope of the invention, other people make some non-intrinsically safes according to the content of foregoing invention
Change and adjustment, all belong to the scope of protection of the present invention.
It was found by the inventors of the present invention that the preparation method of the sponge of the existing Component units based on graphene is at present still
There is the compressible super-elasticity of omnidirectional, omnidirectional can reply compressibility, high intensity and high conductance for the preparation for not having low cost, controllability good
The method of the carbon sponge of rate.
Fig. 2 is the micro image of carbon sponge according to an embodiment of the invention.As shown in Fig. 2, provided by the invention
Carbon sponge is a kind of composition.It is characterized in that:" brick is passed through by the graphene oxide and amorphous carbon of graphene or partial reduction
Mud " structure constructs to be formed." brick mud " if structure refer to by dried layer graphene or partial reduction graphene oxide be used as " brick ",
Amorphous carbon is coated as " mud " or part coats the graphene or the graphene oxide of partial reduction, so that graphene or portion
Divide porous network shape composite construction of the graphene oxide of reduction with amorphous carbon linking into similar " brick mud " structure.Its component
Weight percent be:Graphene or the graphene oxide 0.1-99.9% of partial reduction, amorphous carbon 0.1%-99.9%.
Further, the carbon sponge formed by graphene and amorphous carbon, consisting of carbon.By the oxygen of partial reduction
The carbon sponge that graphite alkene and amorphous carbon are formed, consisting of oxygen and carbon.Wherein, the oxygen element atomic percent of carbon sponge
When than≤1%, carbon sponge is properly termed as full carbon sponge.
As shown in Fig. 2, carbon sponge is macroscopically porous foam shape.Shape, size and dimension are unlimited.By carbon and oxygen member
Element composition, is free of other elements.Density can be down to 0.25mg/cm3.Ranging from 1.5nm-550 μm of pore size.As Fig. 3-6 institute
Show, excellent elasticity is all had along different directions and compressibility can be replied, that is, has the compressible super-elasticity of omnidirectional and omnidirectional can
Reply compressibility.Compressive strength can be more than 400kPa, and conductivity can be more than 90S/m.
Preferably, the graphene 10%-90% in carbon sponge, amorphous carbon 10%-80%.
Preferably, the graphene 50%-80% in carbon sponge, amorphous carbon 20%-50%.
Preferably, carbon sponge oxygen element atomic percent >=0.01%, remaining all carbon.
Preferably, full carbon sponge oxygen element atomic percent >=0.01% and≤1%, remaining all carbon.
Further, component ratio is arbitrarily adjustable in carbon sponge.
Optionally, the atomic percent of oxygen element can be controlled in 60%-50% in the component of carbon sponge, remaining is complete
Portion is carbon.
Optionally, the atomic percent of oxygen element can be controlled in 50%-20% in the component of the carbon sponge,
Remaining all carbon.
Optionally, the atomic percent of oxygen element can be controlled in 20%-10% in the component of the carbon sponge,
Remaining all carbon.
Optionally, the atomic percent of oxygen element can be controlled in 10%-5% in the component of the carbon sponge,
Remaining all carbon.
Optionally, the atomic percent of oxygen element can be controlled in 5%-3% in the component of the carbon sponge,
Remaining all carbons.
Optionally, the atomic percent of oxygen element can be controlled in 3%-1% in the component of the carbon sponge,
Remaining all carbons.
Optionally, the atomic percent of oxygen element can be controlled in 0.1%- in the component of the full carbon sponge
1%, remaining all carbon.
Optionally, the atomic percent of oxygen element can be controlled in 0%- in the component of the full carbon sponge
0.6%, remaining all carbon.
Optionally, the atomic percent of oxygen element can be controlled in 0%- in the component of the full carbon sponge
0.1%, remaining all carbon.
Optionally, the atomic percent of oxygen element can be controlled in 0.1%- in the component of the carbon sponge
60%, remaining all carbon.
Carbon sponge provided by the invention is ultralight, and density can be down to 0.25mg/cm3.The density of carbon sponge is in a certain range
It is adjustable.For example,
Optionally, the density range of the carbon sponge includes 0.25-0.5mg/cm3。
Optionally, the density range of the carbon sponge includes 0.51-1mg/cm3。
Optionally, the density range of the carbon sponge includes 1-5mg/cm3。
Optionally, the density range of the carbon sponge includes 0.5-3mg/cm3。
Optionally, the density range of the carbon sponge includes 5-15mg/cm3。
Optionally, the density range of the carbon sponge includes 15-30mg/cm3。
Optionally, the density range of the carbon sponge includes 30-50mg/cm3。
Optionally, the density range of the carbon sponge includes 40-50mg/cm3。
Optionally, the density range of the carbon sponge includes 50-100mg/cm3。
Optionally, the density range of the carbon sponge includes 100-200mg/cm3。
The pore diameter range of carbon sponge provided by the invention is adjustable in 1.5nm-550 μm.For example,
Optionally, the pore diameter range of the carbon sponge includes 1.5nm-100nm.
Optionally, the pore diameter range of the carbon sponge includes 1nm-100nm.
Optionally, the pore diameter range of the carbon sponge includes 100nm-10 μm.
Optionally, the pore diameter range of the carbon sponge includes 10 μm -50 μm.
Optionally, the pore diameter range of the carbon sponge includes 50 μm -200 μm.
Optionally, the pore diameter range of the carbon sponge includes 200 μm -250 μm.
Optionally, the pore diameter range of the carbon sponge includes 250 μm -550 μm.
There is carbon sponge provided by the invention the compressible super-elasticity of omnidirectional, omnidirectional can reply compressibility and electric conductivity.Wherein,
The compressible super-elasticity of omnidirectional refers to sponge can be restored to original length when removing pressure after the compression of its any direction.Omnidirectional can return
Compound compression refers to sponge can restore 60% or more of original length when removing pressure after the compression of its any direction.
The strain of the compressible recovery of the compressible super-elasticity of omnidirectional and omnidirectional of carbon sponge provided by the invention exists in range
It is adjustable in 0.1-99.9%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 0.1-
20%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 20-40%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 40%-
60%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 60-80%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 70-90%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 90-
95.9%.
Optionally, the range of strain of the compressible recovery of the compressible super-elasticity of the omnidirectional and omnidirectional includes 96-
99.9%.
Optionally, the strain model of the compressible recovery of the compressible super-elasticity of omnidirectional and omnidirectional of carbon sponge provided by the invention
It encloses including 98.5-99.9%.
As shown in Figure 1, carbon sponge provided by the invention is being in macroscopically the porous foam shape of random geometry.Carbon sponge
It can be processed or be cut into random geometry.For example, the shape of carbon sponge include rule sphere, cube, cylinder,
Polygon cylinder;Irregular solid;Thin slice, the film of arbitrary shape;Fiber and nano wire.On carbon sponge macro-size
It is unlimited, it is most thin up to 1 nanometer.It is unlimited in carbon sponge dimension, including three-dimensional, such as the block shape of random geometry;Two dimension is such as received
Rice piece, film;It is one-dimensional, as nanofiber, nanometer are linear;Zero dimension, such as nanosphere.
Further, carbon sponge provided by the invention has the characteristics that ultralight and high intensity.Carbon sponge can be born to reach itself
Several weights of weight compress and keep its structural intergrity.The time equal energy of density, graphene and amorphous carbon ratio, heat treatment
The ratio of (finger pressure contracting can be born and keep its structural intergrity) weight quality and own wt that can be born of regulation and control sponge.
Preferably, the ratio of the weight quality and own wt that can bear of carbon sponge is up to 150,000 or more.
Preferably, the ratio of the weight quality and own wt that can bear of the carbon sponge is smaller than equal to 0.8 ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge includes 0.8 ten thousand -5
Ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge includes 5.1 ten thousand -10
Ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge includes 100,000-20
Ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge up to 100,000 with
On.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge includes 200,000-50
Ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge includes 300,000-50
Ten thousand.
Preferably, the range of the ratio of the weight quality and own wt that can bear of the carbon sponge up to 300,000 with
On.
As shown in figure 14, the present invention also provides a kind of preparation methods of the compressible super-elasticity carbon sponge of omnidirectional, including with
Lower step:
Additive and graphene oxide are distributed to formation graphene oxide and additive mixed solution in solvent by step 1.
The mixed solution is dried step 2, obtains the graphene oxide sponge containing additive.
Step 3, under inert gas protection high-temperature heat treatment graphene oxide containing additive sponge, obtain carbon sponge or
Full carbon sponge.
Specifically, additive is one or more of small molecular organic acid.Preferably, additive is ascorbic acid, lemon
Lemon acid, tartaric acid, lactic acid, one or more of benzoic acid.Solvent be for the water of dispersing additive and graphene oxide and
Organic solvent.Preferably, solvent is the mixing of one or more of water, ethyl alcohol, acetone, dimethylformamide, carbon tetrachloride
Liquid.Drying means for the dry mixed solution containing additive and graphene oxide is freeze-drying, supercritical drying, vacuum
One or more of dry and normal pressure heated drying.The temperature range of high-temperature heat treatment is unlimited, and the time of high-temperature heat treatment is unlimited.
Preferably, the temperature range of high-temperature heat treatment is 200 DEG C -2500 DEG C.Preferably, the time of high-temperature heat treatment is 0.1-100h.
Further, in the high-temperature heat treatment process, using higher heat treatment temperature and longer heat treatment when
Between be conducive to obtain higher reducing degree and the carbon sponge compared with low oxygen content, even without the full carbon sponge of oxygen.
Preferably, the carbon sponge includes the carbon sponge slightly restored, and the atomic percent proportion of oxygen element is 10%-
60%.
Preferably, the carbon sponge includes the carbon sponge of moderate reduction, and the atomic percent proportion of oxygen element is 1%-
10%.
Preferably, the carbon sponge includes the carbon sponge of height reduction, and the atomic percent proportion of oxygen element is 0.5%-
1%.
Preferably, the carbon sponge includes the carbon sponge of high degree reduction, and the atomic percent proportion of oxygen element is≤
0.5%.
Further, the carbon sponge has " brick mud " structure.Described " brick mud " structure refers to by single layer to several layers of
Graphene sheet layer is used as " brick ", and the amorphous carbon that additive pyrolysis generates is as similar " brick mud " structure made of " mud " linking
Porous network shape composite construction.
Further, the carbon sponge have the compressible super-elasticity of omnidirectional, omnidirectional can reply compressibility, high intensity and it is high
Electric conductivity.
There is carbon sponge the principle of above structure and property to be:By preparation method step 2, additive is coated as " mud "
Or part is coated on the surface of graphene oxide layer, while being attached to the gap between graphene oxide layer and lamella
Place.Since additive has weak reduction, graphene oxide slightly to be restored, oxygen content reduces;Portions additive is aoxidized, greatly
Portions additive keeps original structure constant.Since the graphene oxide defect slightly restored is more, it is excellent not have graphene
Power electrical property, so the slight redox graphene sponge containing additive obtained at this time does not have elasticity, when compression, can be sent out
Raw plastic deformation is pressed into powder;Intensity is low and electric conductivity is poor.After step 3 heat treatment, as the slight of " brick "
The graphene oxide of reduction continues the graphene oxide for being reduced into graphene or being partially reduced;And additive is pyrolyzed and
Carbonization generates amorphous carbon, and the graphene oxide sheet of reduction or partial reduction is either partly coated on as " mud " cladding
The surface of layer (being usually also simply referred to as graphene sheet layer), while filling is either partially fill in the oxygen of reduction or partial reduction
At gap between graphite alkene lamella and lamella;Form " brick mud " structure.Complete step 3, when temperature is down to room temperature, " brick mud "
Structure is maintained, and obtains the carbon sponge (including full carbon sponge) of above structure and property.Above-mentioned knot of the additive to carbon sponge
The formation of structure and property has played key effect.Additive but the oxygen reduction Jing Guo same steps 1 and 2,3 processing procedures is not used
Graphite alkene sponge (being usually also referred to as graphene sponge) does not have " adobe " structure, reduction or partial reduction graphene film
Layer is without cladding amorphous carbon, without filling amorphous carbon between lamella;Do not have a super-elasticity, plasticity shape can occur for when compression
Become, intensity is low;But there is certain electric conductivity.It is of the present invention to have compared with this kind of redox graphene sponge
Mechanical property in the carbon sponge (including full carbon sponge) of " brick mud " structure at graphene sheet layer and node significantly increases, network
Electric conductivity greatly improves." brick mud " structural carbon sponge (including full carbon sponge) of the present invention not only has the compressible superlastic of omnidirectional
Property, the compressible recovery of omnidirectional, and its intensity and conductivity are much larger than other carbon sponges prepared with graphene oxide.Its
In, cladding can be that full cladding or part coat.
Compared to the prior art the present invention has the advantage that:
(1) compared with template vapour deposition process, the method that the present invention prepares carbon sponge does not need the step of chemical vapor deposition
Suddenly, therefore complicated chemical vapor depsotition equipment is not needed, preparation method is simple and direct, at low cost.Template vapour deposition process utilizes more
Mesoporous metal is as substrate deposition graphene, so its microstructure depends on the structure of porous metals, is formed for tubular graphene alkene
Network;And the composite construction that " brick mud " structural carbon sponge prepared by the present invention is made of sheet graphene and amorphous carbon
Network can also be obtained by curling graphene film stratiform in the case of but unclosed be formed at tubular graphene alkene and amorphous carbon
Composite construction carbon sponge network;The microstructure and constituent of the two have very big difference.
(2) compared with existing solution self-assembly method, " brick mud " structural carbon sponge prepared by the present invention be by graphene and
The constituent of pyrogenous origin amorphous carbon composition and existing solution self-assembly method, i.e., by macromolecule and graphene, graphite
Graphene is different with carbon nanotube or only for alkene.Due to strong between amorphous carbon and graphene in " brick mud " structure of the present invention
The synergistic effect that generates of π-π interaction, keep prepared carbon sponge porous network firmer, it is compressible to be provided with omnidirectional
Super-elasticity and omnidirectional can reply compressibility, and intensity and conductivity are far longer than sponge prepared by existing solution self-assembly method.
(3) with the method for pyrolysis chitosan and graphene oxide mixture (Nature Communications, 2016,7,
12920) it compares, carbon sponge element group prepared by the present invention becomes carbon and part oxygen element, and is pyrolyzed chitosan and oxidation
The composition of sponge prepared by the method for graphene mixture not only contains carbon and oxygen element and also contains 6% nitrogen, so
The two constitution element component difference is very big.The additive that present invention preparation sponge uses is the organic acid of small molecule, and pyrolysis shell
The polymer chitosan that the method for glycan and graphene oxide mixture uses has difference substantially.The preparation process of the present invention
In mixing liquid need not be processed with liquid nitrogen.Carbon sponge network prepared by the present invention is firmer, has omnidirectional's super-elasticity
Compressibility can be replied with omnidirectional, intensity and conductivity are far longer than the sponge of above method preparation.
(4) the carbon sponge of the composite network structure of the graphene and amorphous carbon with " adobe structure " described in, has
The compressible super-elasticity of omnidirectional, omnidirectional can reply compressibility, high intensity and high conductivity, can be used to construct Novel pressure-resistant contracting it is soft
The electronics devices such as property battery, ultracapacitor, sensor, brake.Also carbon biological tissue holder, ultralight machinery resistance be can be used as
Buddhist nun's porous material and ultralight heat/sound insulation porous material.
Specific embodiment 1:
The graphene oxide of 15 mass parts and 45 mass parts citric acids are distributed to shape in the water of 400 mass parts by step (a)
At graphene oxide and addition agent dispersing liquid.
Graphene oxide and citric acid dispersion liquid injection hollow sphere mold are freeze-dried by step (b), in obtaining
Empty graphene oxide sponge of the spherical shape containing additive.
Step (c) is by graphene oxide sponge of the hollow sphere containing additive under nitrogen atmosphere protection at 400 DEG C at heat
4h is managed, hollow sphere carbon sponge is obtained.
The hollow sphere carbon sponge graphene that this method obtains accounts for 45%, and amorphous carbon accounts for 55%.Original shared by oxygen element
Sub- percentage is 15%, for the carbon sponge slightly restored.It is provided with super-elasticity in all directions, replying on different directions
Compression strain is 90%-99%.Intensity is more than 450kPa.Density is 8.5mg/cm3, conductivity is more than 95S/m.The weight that can be born
The ratio of amount of substance and own wt is 1.5 ten thousand.It is compared with the graphene sponge of composite carbon nanometer tube, PDMS, PPY, this method
The carbon sponge of preparation not only has the compressible super-elasticity of omnidirectional, and intensity and conductivity are more excellent.
In the present embodiment, additive is small molecular organic acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Dispersion
Agent can be water and organic solvent;Heat treatment temperature can change within the scope of 200-2500 DEG C;The graphene ratio of obtained carbon sponge
Example is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%-60%, remaining element is carbon, is free of
Other elements;Can recovery strain adjustable in 0.1-99.9%;Density is a wide range of interior adjustable, it is preferable that density exists
0.25mg/cm3-200mg/cm3It is adjustable in range.
Specific embodiment 2:
The graphene oxide of 45 mass parts is distributed in the water of 450 mass parts by step (a) to be formed graphene oxide and adds
Add agent dispersing liquid.
Graphene oxide dispersion injection cuboid mold is carried out supercritical drying by step (b), obtains cuboid
Graphene oxide sponge, the ratio shared by additive are 0%, and the ratio shared by graphene oxide is 100%.
Cuboid graphene oxide sponge is heat-treated 4h by step (c) under nitrogen atmosphere protection at 800 DEG C, is grown
Cube shape carbon sponge.
The carbon sponge graphene that this method obtains accounts for 100%, is free of amorphous carbon.Atomic percent shared by oxygen element is
60%, for the carbon sponge slightly restored.Do not have super-elasticity, can recovery strain amount be 0%, density 3.5mg/cm3.Conductance is small
In 70S/m.
In the present embodiment, additive is small molecular organic acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Dispersion
Agent can be water and organic solvent;Heat treatment temperature can change within the scope of 200-2500 DEG C;The graphene ratio of obtained carbon sponge
Example is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%-60%, remaining element is carbon, is free of
Other elements;Can recovery strain adjustable in 0.1-99.9%;Density is a wide range of interior adjustable, it is preferable that density exists
0.25mg/cm3-200mg/cm3It is adjustable in range.
Specific embodiment 3
45 mass parts ascorbic acid of step (a), which is distributed in 400 mass parts ethyl alcohol, forms graphene oxide and additive point
Dispersion liquid.
The injection of step (b) ascorbic acid dispersion liquid is spherical to carry out supercritical drying, obtains spherical ascorbic acid sponge addition
Ratio shared by agent is 100%, and the ratio shared by graphene oxide is 0%.
Spherical ascorbic acid sponge is heat-treated 0.4h by step (c) under nitrogen atmosphere protection at 900 DEG C, obtains spherical carbon
Sponge.
Amorphous carbon accounts for 100% in the spherical sponges that this method obtains, not graphene-containing.Atomic percent shared by oxygen element
Than being 45%, for the carbon sponge slightly restored.Be not provided with super-elasticity, can recovery strain amount be 0%, density 3.5mg/cm3。
Conductivity is less than 100S/m.
In the present embodiment, additive is small molecular organic acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Dispersion
Agent can be water and organic solvent;Heat treatment temperature can change within the scope of 200-2500 DEG C;The graphene ratio of obtained carbon sponge
Example is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%-60%, remaining element is carbon, is free of
Other elements;Can recovery strain adjustable in 0.1-99.9%;Density is a wide range of interior adjustable, it is preferable that density exists
0.25mg/cm3-200mg/cm3It is adjustable in range.
Specific embodiment 4:
The graphene oxide of 50 mass parts and 5 mass parts ascorbic acid are distributed to the dimethyl of 300 mass parts by step (a)
Graphene oxide and addition agent dispersing liquid are formed in formamide.
Graphene oxide and ascorbic acid dispersion liquid injection film shape mold are freeze-dried by step (b), obtain ball
Graphene oxide sponge of the hull shape containing additive.
Graphene oxide sponge of the film shape containing additive is heat-treated under nitrogen atmosphere protection at 900 DEG C by step (c)
2h obtains film shape carbon sponge.
The film shape carbon sponge graphene that this method obtains accounts for 45%, and amorphous carbon accounts for 55%.Atom shared by oxygen element
Percentage is 9%, for the carbon sponge of moderate reduction.It is provided with super-elasticity in all directions, pressure is replied on different directions
Shrinkage strain is 60%-89%.Intensity is more than 500kPa.The ratio of the weight quality and own wt born is 100,000.Density is
17mg/cm3, conductivity is more than 100S/m.It is compared with the graphene sponge of composite carbon nanometer tube, PDMS, PPY, prepared by this method
Carbon sponge not only have the compressible super-elasticity of omnidirectional, intensity and conductivity are more excellent.
In the present embodiment, additive is small molecular organic acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Dispersion
Agent can be water and organic solvent;Heat treatment temperature can change within the scope of 200-2500 DEG C;The graphene ratio of obtained carbon sponge
Example is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%-60%, remaining element is carbon, is free of
Other elements;Can recovery strain adjustable in 0.1-99.9%;Density is a wide range of interior adjustable, it is preferable that density exists
0.25mg/cm3-200mg/cm3It is adjustable in range.
Specific embodiment 5:
The graphene oxide of 50 mass parts and 50 mass parts tartaric acid are distributed to shape in the water of 5000 mass parts by step (a)
At graphene oxide and addition agent dispersing liquid.
Graphene oxide and the spherical shape mold of tartaric acid dispersion liquid injection are freeze-dried by step (b), are obtained cube
Graphene oxide sponge of the bodily form containing additive.
Graphene oxide sponge of the spherical shape containing additive is heat-treated 4h by step (c) under nitrogen atmosphere protection at 500 DEG C,
Obtain spherical carbon sponge.
The spherical carbon sponge graphene that this method obtains accounts for 20%, and amorphous carbon accounts for 80%.Atom hundred shared by oxygen element
Divide than being 35%, for the carbon sponge of moderate reduction.It is provided with super-elasticity in all directions, compression is replied on different directions
Strain is 60%-89%.Intensity is more than 520kPa.Density is 9.3mg/cm3, conductivity is more than 85S/m.The weight quality born
Ratio with own wt is 220,000.It is compared with the graphene sponge of composite carbon nanometer tube, PDMS, PPY, carbon prepared by this method
Sponge not only has the compressible super-elasticity of omnidirectional, and intensity and conductivity are more excellent.
In this present embodiment, additive is small molecular organic acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Point
Powder can be water and organic solvent;Heat treatment temperature can change within the scope of 200-2500 DEG C;The graphene of obtained carbon sponge
Ratio is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%-60%, remaining element is carbon, no
Containing other elements;Can recovery strain adjustable in 0.1-99.9%;Density is a wide range of interior adjustable, it is preferable that density exists
0.25mg/cm3-200mg/cm3It is adjustable in range.
Specific embodiment 6:
The graphene oxide of 45 mass parts and 15 mass parts citric acids are distributed to shape in the water of 400 mass parts by step (a)
At graphene oxide and addition agent dispersing liquid.
Graphene oxide and citric acid dispersion liquid injection cylindrical die are freeze-dried by step (b), obtain cylinder
Graphene oxide sponge of the shape containing additive.
Graphene oxide sponge containing cylindrical additive is heat-treated under nitrogen atmosphere protection at 900 DEG C by step (c)
14h obtains cylindrical carbon sponge.
The cylindrical carbon sponge graphene that this method obtains accounts for 25%, and amorphous carbon accounts for 57%.Atom shared by oxygen element
Percentage is 15%, for the carbon sponge of moderate reduction.It is provided with super-elasticity in all directions, pressure is replied on different directions
Shrinkage strain is 65%-95%.Intensity is more than 500kPa.Density is 4.3mg/cm3, conductivity is more than 80S/m.The heavy substance born
The ratio of amount and own wt is 350,000.It is compared with the graphene sponge of composite carbon nanometer tube, PDMS, PPY, prepared by this method
Carbon sponge not only has the compressible super-elasticity of omnidirectional, and intensity and conductivity are more excellent.
In the present embodiment, additive is small molecular organic acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Dispersion
Agent can be water and organic solvent;Heat treatment temperature can change within the scope of 200-2500 DEG C;The graphene ratio of obtained carbon sponge
Example is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%-60%, remaining element is carbon, is free of
Other elements;Can recovery strain adjustable in 0.1-99.9%;Density is a wide range of interior adjustable, it is preferable that density exists
0.25mg/cm3-200mg/cm3It is adjustable in range.
Specific embodiment 7:
The graphene oxide of 50 mass parts and 40 mass parts lactic acid are distributed in the water of 400 mass parts and are formed by step (a)
Graphene oxide and addition agent dispersing liquid.
Graphene oxide and lactic acid dispersion liquid injection I font molds are freeze-dried by step (b), are obtained flower bed shape and are contained
The graphene oxide sponge of additive.
Graphene oxide sponge of the I fonts containing additive is heat-treated under nitrogen atmosphere protection at 1200 DEG C by step (c)
40h obtains I font carbon sponges.
The I font carbon sponge graphenes that this method obtains account for 65%, and amorphous carbon accounts for 35%.Atom hundred shared by oxygen element
Divide the carbon sponge than being 0.2%, restored for high degree.It is provided with super-elasticity in all directions, replying on different directions
Compression strain is 95%-99%.Intensity is more than 700kPa.Density is 45mg/cm3, conductivity is more than 100S/m.The weight born
The ratio of quality and own wt is 400,000.It is compared with the graphene sponge of composite carbon nanometer tube, PDMS, PPY, prepared by this method
Carbon sponge not only have the compressible super-elasticity of omnidirectional, intensity and conductivity are more excellent.
In the present embodiment, additive is small molecular organic acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Dispersion
Agent can be water and organic solvent;Heat treatment temperature can change within the scope of 200-2500 DEG C;The graphene ratio of obtained carbon sponge
Example is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%-60%, remaining element is carbon, is free of
Other elements;Can recovery strain adjustable in 0.1-99.9%;Density is a wide range of interior adjustable, it is preferable that density exists
0.25mg/cm3-200mg/cm3It is adjustable in range.
Specific embodiment 8:
The graphene oxide of 15 mass parts and 15 mass parts benzoic acid are distributed to shape in the water of 400 mass parts by step (a)
At graphene oxide and addition agent dispersing liquid.
Graphene oxide and benzoic acid dispersion liquid injection O font molds are dried in vacuo by step (b), obtain O fonts
Graphene oxide sponge containing additive.
Graphene oxide sponge of the O fonts containing additive is heat-treated under nitrogen atmosphere protection at 1700 DEG C by step (c)
400h obtains O font carbon sponges.
The O font carbon sponge graphenes that this method obtains account for 25%, and amorphous carbon accounts for 75%.Atom hundred shared by oxygen element
Divide the carbon sponge than being 0.01%, restored for high degree.It is provided with super-elasticity in all directions, replying on different directions
Compression strain is 55%-83%.Intensity is more than 690kPa.Density is 15mg/cm3, conductivity is more than 80S/m.The weight born
The ratio of quality and own wt is 450,000.It is compared with the graphene sponge of composite carbon nanometer tube, PDMS, PPY, prepared by this method
Carbon sponge not only have the compressible super-elasticity of omnidirectional, intensity and conductivity are more excellent.
In the present embodiment, additive is small molecular organic acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Dispersion
Agent can be water and organic solvent;Heat treatment temperature can change within the scope of 200-2500 DEG C;The graphene ratio of obtained carbon sponge
Example is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%~60%, remaining element is carbon, is free of
Other elements;Can recovery strain adjustable in 0.1-99.9%;Density is a wide range of interior adjustable, it is preferable that is more than 0.5mg/
cm3。
Specific embodiment 9:
The graphene oxide of 25 mass parts and 25 mass parts benzoic acid are distributed to the dimethyl of 500 mass parts by step (a)
Graphene oxide and addition agent dispersing liquid are formed in formamide.
Graphene oxide and benzoic acid dispersion liquid are injected cube shaped mold and carry out common heated drying by step (b), are obtained
The cube shaped graphene oxide sponge containing additive.
Step (c) is by the cube shaped graphene oxide sponge containing additive under nitrogen atmosphere protection at 800 DEG C at heat
4h is managed, carbon sponge is obtained.
The cube shaped carbon sponge graphene that this method obtains accounts for 60%, and amorphous carbon accounts for 40%.Original shared by oxygen element
Sub- percentage is 35%, for the carbon sponge slightly restored.It is provided with super-elasticity in all directions, replying on different directions
Compression strain is 85%-99.5%.Intensity is more than 700kPa.Density is 0.5mg/cm3, conductivity is more than 100S/m.It bears
The ratio of weight quality and own wt is 100.It is compared with the graphene sponge of composite carbon nanometer tube, PDMS, PPY, this method
The carbon sponge of preparation not only has the compressible super-elasticity of omnidirectional, and intensity and conductivity are more excellent.
In the present embodiment, additive is small molecular organic acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Dispersion
Agent can be water and organic solvent;Heat treatment temperature can change within the scope of 200-2500 DEG C;The graphene ratio of obtained carbon sponge
Example is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%-60%, remaining element is carbon, is free of
Other elements;Can recovery strain adjustable in 0.1-99.9%;Density is a wide range of interior adjustable, it is preferable that density exists
0.25mg/cm3-200mg/cm3It is adjustable in range.
Specific embodiment 10:
The graphene oxide of 45 mass parts and 45 mass parts ascorbic acid are distributed to the ethyl alcohol of 500 mass parts by step (a)
Middle formation graphene oxide and addition agent dispersing liquid.
Graphene oxide and ascorbic acid dispersion liquid injection film shape mold are carried out supercritical drying by step (b), are obtained
Graphene oxide sponge of the film shape containing additive.
Graphene oxide sponge of the film shape containing additive is heat-treated under nitrogen atmosphere protection at 550 DEG C by step (c)
4h obtains film shape carbon sponge.
The film shape carbon sponge graphene that this method obtains accounts for 85%, and amorphous carbon accounts for 15%.Atom shared by oxygen element
Percentage is 35%, for the carbon sponge slightly restored.It is provided with super-elasticity in all directions, pressure is replied on different directions
Shrinkage strain is 85%-87%.Intensity is more than 750kPa.Density is 2.5mg/cm3, conductivity is more than 75S/m.The heavy substance born
The ratio of amount and own wt is 30,000.It is compared with the graphene sponge of composite carbon nanometer tube, PDMS, PPY, prepared by this method
Carbon sponge not only has the compressible super-elasticity of omnidirectional, and intensity and conductivity are more excellent.
In the present embodiment, additive is small molecular organic acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Dispersion
Agent can be other solvents;Heat treatment temperature can change within the scope of 200-2500 DEG C;The graphene ratio of obtained carbon sponge exists
It is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%~60%, remaining element is carbon, without other
Element;Can recovery strain adjustable in 0.1-99.9%;Density is a wide range of interior adjustable, it is preferable that density is in 0.25mg/
cm3-200mg/cm3It is adjustable in range.
Specific embodiment 11:
The graphene oxide of 85 mass parts and 100 mass tartaric acid are distributed to shape in the ethyl alcohol of 400 mass parts by step (a)
At graphene oxide and addition agent dispersing liquid.
Graphene oxide and tartaric acid dispersion liquid injection hexagonal cylindrical mold are carried out heated drying by step (b), obtain hexagonal
Graphene oxide sponge of the cylindricality containing additive.
Step (c) is by graphene oxide sponge of the hexagonal cylindricality containing additive under nitrogen atmosphere protection at 950 DEG C at heat
4h is managed, hexagonal cylindricality carbon sponge is obtained.
The hexagonal cylindricality carbon sponge graphene that this method obtains accounts for 80%, and amorphous carbon accounts for 20%.Original shared by oxygen element
Sub- percentage is 13%, for the carbon sponge of moderate reduction.It is provided with super-elasticity in all directions, replying on different directions
Compression strain is 60%-94%.Intensity is more than 450kPa.Density is 3.5mg/cm3, conductivity is more than 90S/m.The weight born
The ratio of quality and own wt is 20,000.It is compared with the graphene sponge of composite carbon nanometer tube, PDMS, PPY, prepared by this method
Carbon sponge not only have the compressible super-elasticity of omnidirectional, intensity and conductivity are more excellent.
In the present embodiment, additive is small molecular organic acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Dispersion
Agent can be other solvents;Heat treatment temperature can change within the scope of 200-2500 DEG C;The graphene ratio of obtained carbon sponge exists
It is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%-60%, remaining element is carbon, without other
Element;Can recovery strain adjustable in 0.1-99.9%;Density is a wide range of interior adjustable, it is preferable that density is in 0.25mg/
cm3-200mg/cm3It is adjustable in range.
Specific embodiment 12:
The graphene oxide of 50 mass parts and 50 mass parts ascorbic acid are distributed in the water of 500 mass parts by step (a)
Form graphene oxide and addition agent dispersing liquid.
Graphene oxide and the spherical shape mold of ascorbic acid dispersion liquid injection are carried out supercritical drying by step (b), are obtained
Graphene oxide sponge of the spherical shape containing additive.
Graphene oxide sponge of the spherical shape containing additive is heat-treated under nitrogen atmosphere protection at 1200 DEG C by step (c)
4h obtains spherical carbon sponge.
Step (d) cuts spherical carbon sponge, obtains the two-dimensional slice stratiform carbon sponge that thickness is 1nm.
The two-dimensional slice stratiform carbon sponge graphene that this method obtains accounts for 95%, and amorphous carbon accounts for 5%.Original shared by oxygen element
Sub- percentage is 0.8%, for the carbon sponge of height reduction.Direction is provided with super-elasticity along piece level, along different directions
It is 98%-99.9% that compression strain, which can be replied,.Intensity is more than 100kPa.Density is 0.2mg/cm3, conductivity is more than 50S/m.It holds
The ratio of the weight quality and own wt received is 100.It is compared with the graphene sponge of composite carbon nanometer tube, PDMS, PPY, this
Carbon sponge prepared by method not only has the compressible super-elasticity of omnidirectional, and intensity and conductivity are more excellent.
In other embodiments provided by the invention, additive is small molecular organic acid;The ratio of additive and graphene oxide
Example is arbitrary adjustable;Dispersant can be other solvents;Heat treatment temperature can change within the scope of 200-2500 DEG C;Obtained carbon sponge
Graphene ratio it is adjustable within the scope of 10%-90%;The ratio of oxygen element is adjustable in 0.1%-60%, remaining element is carbon
Element is free of other elements;Can recovery strain adjustable in 0.1-99.9%;Density is adjustable in wide range, it is preferable that
Less than 200mg/cm3。
The present invention also provides a kind of tactile and pressure sensor, it can be used for detecting the tactile and pressure of carbon sponge any direction
Power;Its structure is:Foregoing carbon sponge 4, the electrode 1 (3) contacted with carbon sponge 4 and measuring electrode 1 (3) and carbon sponge
The measuring device 2 of electric signal between 4.Preferably, carbon sponge 4 is the compressible super-elasticity carbon sponge of omnidirectional.
Specifically, the compressible super-elasticity carbon sponge of omnidirectional can be arbitrary shape, can be processed or be cut into arbitrary shape.
Preferably, it can be sphere, cube, cylinder, polygon cylinder;Irregular solid;The thin slice of arbitrary shape, film or
Person's fiber.
Electrode 1 (3) refers to the conductive material not chemically reacted with carbon sponge 4.Preferably, the metals such as gold, silver, copper and
The electrode for the rigidity that its compound is constituted;Carbon nanotube, metal nanometer line, loads electrically conducting transparent on a flexible substrate at graphene
The preferable electrode of flexibility that oxide, conducting polymer and its compound are constituted.The not limited to of electrode 1 (3).Electrode 1 (3)
Position is unlimited, can be symmetrically placed or be asymmetrically placed.Electrode position is unlimited, can be placed on inside carbon sponge either table
Face.
Optionally, there is no any binders or mechanical connection to fix for the contact interface between electrode and carbon sponge.
Further, the electric signal of the output of sensor is unlimited.In the particular embodiment, the electric signal of sensor output
Can be electric current, voltage, resistance.
Further, sensor is used as work materials by using different carbon sponges 4, and tactile and pressure sensor have
Different detection limits and working range.
Optionally, sensor includes being directed to small pressure, and detection limit is less than or equal to the touch sensor of 15Pa.
Optionally, sensor includes being directed to middle pressure, and detection limit is less than or equal to the touch sensor of 50Pa.
Optionally, sensor includes being directed to smaller pressure, and working range is 15Pa-200Pa pressure sensors.
Optionally, sensor includes being directed to middle pressure, and working range is the pressure sensor of 200Pa-10kPa.
Optionally, sensor includes being directed to middle pressure, and working range is the pressure sensor of 100Pa-5kPa.
Optionally, sensor includes being directed to big pressure, and working range is the pressure sensor more than 10kPa.
Optionally, sensor includes being directed to big pressure, and working range is the pressure sensor more than 100kPa.
Tactile provided by the invention and pressure sensor be based on above-mentioned carbon sponge it is a kind of can omnidirectional's detection pressure, visit
Survey the low and highly sensitive sensor of lower limit.
The signals such as pressure, temperature, strain are changed into electric signal, being can by the function of electronic skin energy natural imitation skin
One of the important directions of wearable device development.Carbon material is to prepare high-performance sensors due to its good flexible and electric conductivity
Work materials.Existing tactile and pressure sensor, based on only having unidirectional hyperelastic conductive porous material, such as high temperature reduction
Stone prepared by the graphene sponge (Kuang, J., et al., Nanoscale, 2013,5,12171-7) of preparation, ice crystal template
Black alkene sponge (Qiu, L., et al., Nature communication, 2012,3,7), cannot achieve in multiple directions or even
Pressure detection on all directions.Further, what existing tactile and pressure sensor working mechanism utilized is the body of material
The phenomenon that piezoresistive effect, i.e. bulk resistor are with change in pressure.The limitation of receptor piezoresistive effect, the right linearity of sensors with auxiliary electrode
Good, convenient signal treatment, but the minimum pressure that can be detected, that is, detection limit excessively high (about 100Pa, and 10Pa or so
Touching gently in corresponding people's tactile, institute's sensors with auxiliary electrode can not be comparable with the natural skin tactile detection limit of people), spirit
Sensitivity is very low (being less than 0.01/kPa).So there has been no can the detectable pressure of omnidirectional, detection limit it is low and highly sensitive
Tactile and pressure sensor.
The present invention provides a kind of pressure sensor, can be used for detecting the pressure of carbon aerogels any direction;Its structure is:Such as
Electric signal measurement device between the preceding carbon aerogels, electrode and the measurement electrode and carbon aerogels.Aeroge and
There are conductive silver glues between electrode, for eliminating influence of the contact resistance for signal.
The wherein pressure sensor, using bulk resistor effect as its sensor mechanism, detection power range is big, sensitivity
Higher, low energy consumption, and stability is good, the pressure on detectable any direction.
Tactile provided by the invention and pressure sensor, using interface contact resistance effect rather than body piezoresistive effect conduct
Sensor mechanism, detection power lower limit is up to less than or equal to 15Pa (touching gently in the corresponding people's tactiles of 10Pa or so), sensitivity
Up to 100/kPa, energy consumption are less than 30 μ W.
Preferably, the tactile and pressure sensor use conductive carbon material as electrode and conducting wire, obtained sensing
Device is full carbon tactile and pressure sensor.Full carbon tactile and pressure sensor Ultra light-weight.Full carbon tactile and pressure sensor energy
It works under extreme environment.Operating temperature range is wide, can be worked normally under extremely low temperature;The corrosion of acid and alkali resistance and salt.
Compared to the prior art the present invention has the advantage that:
Based on omnidirectional compressible super-elasticity, high intensity and the carbon sponge of high conductivity can detect along any direction
The tactile and pressure sensor of pressure not only expand the working range of sensor and improve ability to work, reduce sensor
Cost of layout.Its detection limit is low, high sensitivity, is suitable as the tactile of the monitoring and mechanical bionic hand of health signal
Sensor.Particularly, when using conductive carbon materials such as carbon nanotube or graphenes as electrode and conducting wire, full carbon can be prepared
Sensor.The sensor of full carbon has the characteristics that wide light weight, operating temperature range, acid and alkali-resistance and salt corrosion, aerospace,
The special occasion for needing tactile and pressure detection such as strong corrosive environment is with a wide range of applications.
Tactile provided by the invention and pressure sensor, specifically example are as follows:
Specific embodiment 13
As shown in fig. 7, step a) prepares spherical carbon sponge, it is made of above-mentioned preparation sponge method.
Step b) arranges center copper electrode on spherical shaped elastomeric carbon sponge, sponge surface arrange one can be in any direction
Movable free electrode, can the detection of three dimensional spatially pressure on any direction.
It obtains being the touch sensor for middle pressure, working range is more than 100kPa, and sensitivity is up to 2/
KPa, energy consumption are less than 30 μ W, the pressure on detectable three dimensions on any direction.
Wherein, in the figure 7,5 be any direction a direction vector;6 be throwing of the direction vector in XOY plane
Shadow;7 be the angle of direction vector sum Z axis;8 project and the angle of X-axis positive direction for direction vector in XOY plane.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) it is more than 10kPa, 7) it is more than 100kPa.It can visit
The number of the pressure of survey can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 14
As shown in figure 8, step a) prepares spherical carbon sponge, it is made of above-mentioned preparation sponge method.
Step b) 4 surface layout of spherical carbon sponge two can movable free electrode 1 (3) in any direction, can visit
Survey the pressure on any direction on three dimensions.
It obtains being the touch sensor for middle pressure, working range is more than 100kPa, and sensitivity is up to 2/
KPa, energy consumption are less than 30 μ W, the pressure on detectable three dimensions on any direction.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) it is more than 10kPa, 7) it is more than 100kPa.Sensitivity
It is adjustable with energy consumption.The electric signal of output can be the one or several kinds in resistance, electric current, voltage.The pressure that can be detected
Number can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 15
As shown in figure 9, step a) prepares cylindrical carbon sponge, it is made of above-mentioned preparation sponge method.
Step b) arranges that the gold electrode 3 of sand paper polishing, area are slightly less than the surface of sponge, phase on cylindrical carbon sponge 4
There are certain intervals between mutually, packet is on the surface of cylinder, and eight altogether, there are one electrodes 1 as fixed electrode, energy in centre
8 sides of detection upward pressure.
It obtains being the touch sensor for middle pressure, working range 15Pa-200Pa, sensitivity is up to 10/
KPa, energy consumption are less than 30 μ W, different power on detectable 8 directions.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa pressure sensors, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) it is more than 10kPa, 7) it is more than
100kPa.Sensitivity and energy consumption are adjustable.The electric signal of output can be the one or several kinds in resistance, electric current, voltage.It can be with
The number of the pressure of detection can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 16
As shown in Figure 10, step a) prepares cylindrical carbon sponge, is made of above-mentioned preparation sponge method.
Step b) arranges that the gold electrode 3 of sand paper polishing, area are slightly less than the surface of sponge, phase on cylindrical carbon sponge 4
There are certain intervals between mutually, packet is on the surface of cylinder, and six altogether, there are one electrodes 1 as fixed electrode, energy in centre
6 sides of detection upward pressure.
It obtains being the touch sensor for middle pressure, working range 15Pa-200Pa, sensitivity is up to 10/
KPa, energy consumption are less than 30 μ W, different power on detectable 6 directions.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa pressure sensors, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) it is more than 10kPa, 7) it is more than
100kPa.Sensitivity and energy consumption are adjustable.The electric signal of output can be the one or several kinds in resistance, electric current, voltage.It can be with
The number of the pressure of detection can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 17
As shown in figure 11, step a) prepares cylindrical carbon sponge 4, is made of above-mentioned preparation sponge method.
Step b) arranges that the gold electrode 3 of sand paper polishing, area are slightly less than the surface of sponge, phase on cylindrical carbon sponge 4
There are certain intervals between mutually, wraps on the surface of cylinder, eight altogether, 8 sides can be detected and upwarded pressure.
It obtains being the touch sensor for middle pressure, working range 15Pa-200Pa, sensitivity is up to 10/
KPa, energy consumption are less than 30 μ W, different power on detectable 8 directions.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa pressure sensors, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) it is more than 10kPa, 7) it is more than
100kPa.Sensitivity and energy consumption are adjustable.The electric signal of output can be the one or several kinds in resistance, electric current, voltage.It can be with
The number of the pressure of detection can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 18
As shown in figure 12, step a) prepares cylindrical carbon sponge 4, is made of above-mentioned preparation sponge method.
Step b) is slightly less than the surface of sponge in the cylindrical gold electrode 3 for playing arrangement sand paper polishing on carbon sponge 4, area,
There are certain intervals between each other, wraps on the surface of cylinder, six altogether, 6 sides can be detected and upwarded pressure.
It obtains being the touch sensor for middle pressure, working range 15Pa-200Pa, sensitivity is up to 10/
KPa, energy consumption are less than 30 μ W, different power on detectable 6 directions.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa pressure sensors, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) it is more than 10kPa, 7) it is more than
100kPa.Sensitivity and energy consumption are adjustable.The electric signal of output can be the one or several kinds in resistance, electric current, voltage.It can be with
The number of the pressure of detection can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 19
As shown in figure 13, step a) prepares film shape carbon sponge 4, is made of above-mentioned preparation sponge method.
Step b) placement of carbon nanotubes membrane electrodes 11 on foamed film carbon sponge 4, area is slightly less than graphene sponge
Surface, each symmetrically placed one or so each symmetrically placed one, can detect the pressure in both direction up and down.
It obtains being the touch sensor for smaller pressure, working range 15Pa-200Pa, sensitivity is up to 10/
KPa, energy consumption are less than 30 μ W, different power in detectable both direction.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa pressure sensors, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) it is more than 10kPa, 7) it is more than
100kPa.Sensitivity and energy consumption are adjustable.The electric signal of output can be the one or several kinds in resistance, electric current, voltage.It can be with
The number of the pressure of detection can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 20
Step a) prepares cube carbon sponge, is made of above-mentioned preparation sponge method.
Step b) arranges that copper electrode, area are slightly less than the surface of graphene sponge on cube carbon sponge, each right up and down
Claim to place one or so each symmetrically placed one, the pressure in both direction can be detected.
It obtains being the touch sensor for big pressure, working range is > 10kPa, and sensitivity is up to 0.1/kPa, energy
It consumes and is less than 30 μ W, the electric signal of different power in detectable both direction, output is voltage.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa pressure sensors, 3) 200Pa-10kPa, 4) 100Pa-5kPa, 5) it is more than 10kPa, 7) it is more than
100kPa.Sensitivity and energy consumption are adjustable.The electric signal of output can be the one or several kinds in resistance, electric current, voltage.It can be with
The number of the pressure of detection can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 21
Step a) prepares cylindrical carbon sponge, is made of above-mentioned preparation sponge method.
Step b) arranges that the silver electrode of sand paper polishing, area are slightly less than the table of graphene sponge on cylindrical carbon sponge
There are certain intervals in face between each other, and packet is on the surface of cylinder, and eight altogether, there are one electrodes as fixed electricity in centre
Pole can detect 8 sides and upward pressure.
It obtains being the pressure sensor for big pressure, working range is > 10kPa, and sensitivity is up to 0.1/kPa, energy
It consumes and is less than 20 μ W, the electric signal of different power on detectable 8 directions, output is resistance.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa pressure sensors, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) it is more than 10kPa, 7) it is more than
100kPa.Sensitivity and energy consumption are adjustable.The electric signal of output can be the one or several kinds in resistance, electric current, voltage.It can be with
The number of the pressure of detection can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 22
Step a) prepares film shape carbon sponge, is made of above-mentioned preparation sponge method.
Step b) arranges that graphene membrane electrode, area are slightly less than the surface of graphene sponge on film-type carbon sponge,
Each symmetrically placed one up and down, the pressure in both direction can be detected.
It obtains being the touch sensor for middle pressure, working range 400Pa-100kPa, sensitivity is up to 20/
KPa, energy consumption are less than 30 μ W, different power in detectable both direction, and the electric signal of output is resistance.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa pressure sensors, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) it is more than 10kPa, 7) it is more than
100kPa.Sensitivity and energy consumption are adjustable.The electric signal of output can be the one or several kinds in resistance, electric current, voltage.It can be with
The number of the pressure of detection can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 23
Step a) prepares cube carbon sponge, is made of above-mentioned preparation sponge method.
Step b) arranges gold electrode on cube carbon sponge, and area is slightly less than the surface of graphene sponge, upper and lower, preceding
Afterwards, symmetrical to place one, the pressure on three symmetry directions can be detected.
It obtains being the touch sensor for small pressure, detection limit≤15Pa, sensitivity is up to 100/kPa, energy
It consumes and is less than 30 μ W, the electric signal of different power in detectable both direction, output is resistance.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa pressure sensors, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) it is more than 10kPa, 7) it is more than
100kPa.Sensitivity and energy consumption are adjustable.The electric signal of output can be the one or several kinds in resistance, electric current, voltage.It can be with
The number of the pressure of detection can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 24
Step a) prepares cube carbon sponge, is made of above-mentioned preparation sponge method.
Step b) arranges that graphene membrane electrode, area are slightly less than the surface of graphene sponge on cube carbon sponge,
Each symmetrically placed one or so each symmetrically placed one up and down, as shown in figure 4, the pressure in both direction can be detected.
It obtains being the full carbon and pressure touch sensor for big pressure, working range is > 100kPa, and sensitivity can
Up to 10/kPa, energy consumption is less than 30 μ W, and different power in detectable both direction, the electric signal of output is voltage.The full carbon
Tactile and pressure sensor Ultra light-weight.It can be worked normally under extremely low temperature.The corrosion of acid and alkali resistance and salt.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be with
For flexible or rigidity electrode;The material of electrode is the other materials that discord carbon sponge chemically reacts, the position of electrode
It is variable with number;Tactile and the working range of pressure sensor are big, optionally, including:1) be less than or equal to 15Pa, 2) be more than
15Pa, 3) 15Pa-200Pa, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) it is more than 10kPa, 7) it is more than 100kPa.Sensitivity
It is adjustable with energy consumption.The electric signal of output can be the one or several kinds in resistance, electric current, voltage.The pressure that can be detected
Number can be arbitrary positive integer, and direction can also be along three dimensions any direction.
Specific embodiment 25
Step a) prepares cylindrical carbon sponge, is made of above-mentioned preparation sponge method.
Step b) arranges that the gold electrode 3 of sand paper polishing, area are slightly less than the surface of sponge, phase on cylindrical carbon sponge 4
There are certain intervals between mutually, packet is on the surface of cylinder, and six altogether, there are one electrodes 1 as fixed electrode, electricity in centre
It is bonded with conductive silver glue between pole and aeroge, 6 sides can be detected and upwarded pressure.
It obtains being for the pressure sensor of the bulk resistor type of middle pressure, working range is big and adjustable, can wrap
100Pa-2kPa is included, sensitivity is big and adjustable, it may include 10/kPa, energy consumption are less than 30 μ W, different on detectable 6 directions
Power.
In other embodiments provided by the invention, carbon sponge can be rule or irregular shape;Electrode can be
Flexible or rigidity electrode;The material of electrode is the other materials that chemically react of carbon sponge of getting along well, the position of electrode with
Number is variable;The working range of pressure sensor is big, optionally, including:1) be less than or equal to 50Pa, 2) be more than 50Pa, 3)
200Pa-10kPa, 4) 100Pa-5kPa, 5) it is more than 10kPa, 6) it is more than 100kPa.Sensitivity and energy consumption are adjustable.The telecommunications of output
Number can be resistance, electric current, the one or several kinds in voltage.The number for the pressure that can be detected can be arbitrary positive integer, side
To can also be along three dimensions any direction.
In other embodiments provided by the invention, additive is that small molecule is organic in the method for preparing carbon sponge
Acid;The ratio of additive and graphene oxide is arbitrarily adjustable;Dispersant can be other solvents;Heat treatment temperature can be in 200-2500
Change within the scope of DEG C;The graphene ratio of obtained carbon sponge is adjustable within the scope of 10%-90%;The ratio of oxygen element exists
Adjustable in 0.1%-60%, remaining element is carbon, is free of other elements;Can recovery strain can in 0.1-99.9%
It adjusts;Density is in 0.25mg/cm3-200mg/cm3It is adjustable in range.In the method for preparing sensor, carbon sponge can be
Rule or irregular shape;Electrode can be flexible or rigidity electrode;The material of electrode is that discord carbon sponge occurs
The other materials of chemical reaction, the position of electrode and number are variable;Tactile and the working range of pressure sensor are big, optionally,
Including:1) be less than or equal to 15Pa, 2) be more than 15Pa, 3) 15Pa-200Pa, 4) 200Pa-10kPa, 5) 100Pa-5kPa, 6) be more than
10kPa, 7) it is more than 100kPa.Sensitivity and energy consumption are adjustable.The electric signal of output can be one kind in resistance, electric current, voltage
Or it is several.The number for the pressure that can be detected can be arbitrary positive integer, and direction can also be along three dimensions any direction.
The present invention provides carbon sponge and preparation method thereof, the pressure sensing based on the sponge preparation is additionally provided
Device, pressure sensor can be bulk resistor type and contact resistance type.The carbon sponge has the compressible super-elasticity of omnidirectional, omnidirectional can
Reply compressibility, high intensity and high conductivity, can be used to construct Novel pressure-resistant contracting flexible battery, ultracapacitor, sensing
The electronics devices such as device, brake.Also can be used as carbon biological tissue holder, ultralight mechanical damping porous material and it is ultralight every
Heat/sound insulation porous material.Not the step of method for preparing carbon sponge does not need chemical vapor deposition, therefore do not need complexity
Chemical vapor depsotition equipment, preparation method is simple and direct, at low cost.Based on the compressible super-elasticity of omnidirectional, high intensity and high conductance
The tactile and pressure sensor that can detect the pressure along any direction of the sponge of rate, not only expand the work model of sensor
Ability to work is enclosed and improved, the cost of layout of sensor is reduced, detection limit is low, high sensitivity, and it is strong to be suitable as human body
The touch sensor of the monitoring of health signal and mechanical bionic hand.Particularly, when using conductive carbon materials such as carbon nanotube or graphenes
When material is as electrode and conducting wire, the sensor of full carbon can be prepared.The sensor of full carbon have light weight, operating temperature range it is wide,
The characteristics of acid and alkali-resistance and salt corrosion, aerospace, strong corrosive environment etc. it is special need tactile and the occasion of pressure detection to have
Have wide practical use.
So far, although those skilled in the art will appreciate that present invention has been shown and described in detail herein multiple shows
Example property embodiment still without departing from the spirit and scope of the present invention, still can according to the present disclosure directly
Determine or derive many other variations or modifications for meeting the principle of the invention.Therefore, the scope of the present invention is understood that and recognizes
It is set to and covers all these other variations or modifications.
Claims (10)
1. a kind of carbon sponge, which is characterized in that pass through " brick by the graphene oxide and amorphous carbon of graphene or partial reduction
Mud " structure constructs to be formed;" the brick mud " is if structure refers to the graphite oxide of the graphene or partial reduction by single layer or dried layer
Alkene is used as " brick ", and amorphous carbon is coated as " mud " or part coats the graphene or the graphene oxide of partial reduction, with
Graphene or the graphene oxide of partial reduction is set to be connected multiple into the porous network shape of similar " brick mud " structure with amorphous carbon
Close structure;The weight percent of its component is:Graphene or the graphene oxide 0.1-99.9% of partial reduction, amorphous carbon
0.1%-99.9%.
2. carbon sponge according to claim 1, which is characterized in that the carbon sea formed by graphene and amorphous carbon
Silk floss, consisting of carbon;The carbon sponge formed by the graphene oxide and amorphous carbon of partial reduction, consisting of oxygen
And carbon;
Wherein, when the oxygen element atomic percent of the carbon sponge≤1%, the carbon sponge is full carbon sponge.
3. carbon sponge according to claim 1, which is characterized in that the carbon sponge has compressible super-elasticity, can return
Compound compression and electric conductivity;
Preferably, there is the carbon sponge the compressible super-elasticity of omnidirectional, omnidirectional can reply compressibility and electric conductivity;
Wherein, the compressible super-elasticity can be restored to original when to refer to the sponge remove pressure after the compression of its any direction
Length;The compressibility of replying can restore original length when to refer to the sponge remove pressure after the compression of its any direction
60% or more.
4. carbon sponge according to claim 1, which is characterized in that the carbon sponge is in macroscopically the more of random geometry
Hole foam-like;The carbon sponge can be processed or be cut into random geometry.
5. a kind of preparation method of compressible super-elasticity carbon sponge, which is characterized in that include the following steps:
Additive and graphene oxide are distributed in solvent and form graphene oxide and additive mixed solution;
The mixed solution is dried, the graphene oxide sponge containing additive is obtained;
High-temperature heat treatment graphene oxide containing additive sponge under inert gas protection obtains carbon sponge or full carbon sponge.
6. preparation method according to claim 5, which is characterized in that the additive is one kind in small molecular organic acid
Or it is several;
Preferably, the additive is ascorbic acid, citric acid, tartaric acid, lactic acid, one or more of benzoic acid.
7. preparation method according to claim 5, which is characterized in that the solvent is for disperseing the additive and described
Graphene oxide;The solvent includes water and organic solvent;Preferably, the solvent is water, ethyl alcohol, acetone, dimethyl formyl
The mixed liquor of one or more of amine, carbon tetrachloride.
8. preparation method according to claim 5, which is characterized in that described to contain additive and graphene oxide for dry
Mixed solution drying means it is unlimited;
Preferably, the drying means be freeze-drying, supercritical drying, vacuum drying and one kind in normal pressure heated drying or
It is several.
9. preparation method according to claim 5, which is characterized in that the temperature range of the high-temperature heat treatment is unlimited, institute
The time for stating high-temperature heat treatment is unlimited;
Preferably, the temperature range of the high-temperature heat treatment is 200-2500 DEG C;
Preferably, the time of the high-temperature heat treatment is 0.1-100h.
10. a kind of tactile and pressure sensor, which is characterized in that can be used for detecting the tactile and pressure of carbon sponge any direction;
Its structure is:The electrode of carbon sponge described in claim 1-9 and the contact of carbon sponge and measure the electrode and carbon sponge it
Between electric signal measuring device.
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110411623A (en) * | 2019-06-26 | 2019-11-05 | 东华大学 | Highly sensitive flexibility piezoresistance sensor, and its preparation method and application |
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CN114685976A (en) * | 2022-04-27 | 2022-07-01 | 苏州博利迈新材料科技有限公司 | High-toughness conductive nylon material and preparation method thereof |
CN115010985A (en) * | 2022-06-23 | 2022-09-06 | 苏州大学 | rGO/PU conductive sponge, preparation method and application thereof |
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Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102718210A (en) * | 2012-07-03 | 2012-10-10 | 新疆大学 | Method for preparing graphene oxide three-dimensional self-assembled aerogel and application of graphene oxide three-dimensional self-assembled aerogel |
WO2013132260A3 (en) * | 2012-03-09 | 2013-12-05 | Bio Nano Consulting | Cross-linked graphene networks |
CN104291329A (en) * | 2014-09-28 | 2015-01-21 | 北京理工大学 | Graphene sponge and preparation method thereof |
KR20150054051A (en) * | 2013-11-08 | 2015-05-20 | 삼화콘덴서공업주식회사 | Manufacturing method for graphene containing carbon aerogel using polyethyleneimine modified graphene oxide solution |
CN104661959A (en) * | 2012-08-23 | 2015-05-27 | 莫纳什大学 | Graphene-based materials |
CN104843676A (en) * | 2014-12-03 | 2015-08-19 | 北汽福田汽车股份有限公司 | Preparation method for graphene aerogel |
CN104953101A (en) * | 2015-06-24 | 2015-09-30 | 上海交通大学 | Method for manufacturing thermal-treated graphene aerogel-loading tin dioxide electrode material |
CN105513832A (en) * | 2015-12-16 | 2016-04-20 | 华南理工大学 | Graphene/porous carbon composite hydrogel, graphene/porous carbon composite aerogel, and preparation methods and applications thereof |
-
2017
- 2017-05-02 CN CN201710302314.0A patent/CN108328596B/en active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013132260A3 (en) * | 2012-03-09 | 2013-12-05 | Bio Nano Consulting | Cross-linked graphene networks |
CN102718210A (en) * | 2012-07-03 | 2012-10-10 | 新疆大学 | Method for preparing graphene oxide three-dimensional self-assembled aerogel and application of graphene oxide three-dimensional self-assembled aerogel |
CN104661959A (en) * | 2012-08-23 | 2015-05-27 | 莫纳什大学 | Graphene-based materials |
KR20150054051A (en) * | 2013-11-08 | 2015-05-20 | 삼화콘덴서공업주식회사 | Manufacturing method for graphene containing carbon aerogel using polyethyleneimine modified graphene oxide solution |
CN104291329A (en) * | 2014-09-28 | 2015-01-21 | 北京理工大学 | Graphene sponge and preparation method thereof |
CN104843676A (en) * | 2014-12-03 | 2015-08-19 | 北汽福田汽车股份有限公司 | Preparation method for graphene aerogel |
CN104953101A (en) * | 2015-06-24 | 2015-09-30 | 上海交通大学 | Method for manufacturing thermal-treated graphene aerogel-loading tin dioxide electrode material |
CN105513832A (en) * | 2015-12-16 | 2016-04-20 | 华南理工大学 | Graphene/porous carbon composite hydrogel, graphene/porous carbon composite aerogel, and preparation methods and applications thereof |
Non-Patent Citations (2)
Title |
---|
CHENGYI HOU ET AL: "Highly Conductive, Flexible, and Compressible All-Graphene Passive Electronic Skin for Sensing Human Touch", 《ADVANCED MATERIALS》 * |
YUHAO LI ET AL: "Fabrication of 3D foam-like hybrid carbon materials of porous carbon/ graphene and its electrochemical performance", 《ELECTROCHIMICA ACTA》 * |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110411623A (en) * | 2019-06-26 | 2019-11-05 | 东华大学 | Highly sensitive flexibility piezoresistance sensor, and its preparation method and application |
CN111256888A (en) * | 2020-03-02 | 2020-06-09 | 吉林大学 | Bionic multilevel structure flexible stress and strain combined sensor and preparation method thereof |
CN114685976A (en) * | 2022-04-27 | 2022-07-01 | 苏州博利迈新材料科技有限公司 | High-toughness conductive nylon material and preparation method thereof |
CN114685976B (en) * | 2022-04-27 | 2023-10-24 | 苏州博利迈新材料科技有限公司 | High-toughness conductive nylon material and preparation method thereof |
CN115010985A (en) * | 2022-06-23 | 2022-09-06 | 苏州大学 | rGO/PU conductive sponge, preparation method and application thereof |
CN115010985B (en) * | 2022-06-23 | 2023-06-23 | 苏州大学 | rGO/PU conductive sponge, preparation method and application thereof |
CN115893388A (en) * | 2023-02-10 | 2023-04-04 | 青岛科技大学 | High-modulus and high-elasticity graphene foam material and preparation method and application thereof |
CN115893388B (en) * | 2023-02-10 | 2024-06-11 | 青岛科技大学 | High-modulus and high-elasticity graphene foam material and preparation method and application thereof |
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CN116514577B (en) * | 2023-05-05 | 2023-10-20 | 天津大学 | Super-elastic precursor ceramic spring for wide temperature range, pressure sensor of super-elastic precursor ceramic spring and preparation method of super-elastic precursor ceramic spring |
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